Furutama Daisuke, Matsuda Shinji, Yamawaki Yosuke, Hatano Saki, Okanobu Ai, Memida Takumi, Oue Hiroshi, Fujita Tsuyoshi, Ouhara Kazuhisa, Kajiya Mikihito, Mizuno Noriyoshi, Kanematsu Takashi, Tsuga Kazuhiro, Kurihara Hidemi
Department of Periodontal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3, Kasumi, Minami-ku, Hiroshima 734-8553, Japan.
Department of Advanced Pharmacology, Daiichi University of Pharmacy, 22-1 Tamagawa-cho, Minami-ku Fukuoka 815-8511, Japan.
Brain Sci. 2020 Sep 27;10(10):679. doi: 10.3390/brainsci10100679.
Periodontal disease (PD) is a risk factor for systemic diseases, including neurodegenerative diseases. The role of the local and systemic inflammation induced by PD in neuroinflammation currently remains unclear. The present study investigated the involvement of periodontal inflammation in neuroinflammation and blood-brain barrier (BBB) disruption. To induce PD in mice (c57/BL6), a ligature was placed around the second maxillary molar. Periodontal, systemic, and neuroinflammation were assessed based on the inflammatory cytokine mRNA or protein levels using qPCR and ELISA. The BBB permeability was evaluated by the mRNA levels and protein levels of tight junction-related proteins in the hippocampus using qPCR and immunofluorescence. Dextran tracing in the hippocampus was also conducted to examine the role of periodontal inflammation in BBB disruption. The TNF-α, IL-1β, and IL-6 levels markedly increased in gingival tissue 1 week after ligation. The IL-6 serum levels were also increased by ligature-induced PD. In the hippocampus, the IL-1β mRNA expression levels were significantly increased by ligature-induced PD through serum IL-6. The ligature-induced PD decreased the claudin 5 expression levels in the hippocampus, and the neutralization of IL-6 restored its levels. The extravascular 3-kDa dextran levels were increased by ligature-induced PD. These results suggest that the periodontal inflammation-induced expression of IL-6 is related to neuroinflammation and BBB disruption in the hippocampus, ultimately leading to cognitive impairment. Periodontal therapy may protect against neurodegenerative diseases.
牙周病(PD)是包括神经退行性疾病在内的全身性疾病的一个风险因素。目前,由PD引发的局部和全身炎症在神经炎症中的作用仍不清楚。本研究调查了牙周炎症在神经炎症和血脑屏障(BBB)破坏中的作用。为了在小鼠(C57/BL6)中诱导PD,在上颌第二磨牙周围放置结扎线。使用qPCR和ELISA,根据炎性细胞因子mRNA或蛋白质水平评估牙周、全身和神经炎症。使用qPCR和免疫荧光,通过海马中紧密连接相关蛋白的mRNA水平和蛋白质水平评估BBB通透性。还在海马中进行了葡聚糖示踪,以研究牙周炎症在BBB破坏中的作用。结扎后1周,牙龈组织中的TNF-α、IL-1β和IL-6水平显著升高。结扎诱导的PD也使血清IL-6水平升高。在海马中,结扎诱导的PD通过血清IL-6显著增加IL-1β mRNA表达水平。结扎诱导的PD降低了海马中claudin 5的表达水平,而中和IL-6可恢复其水平。结扎诱导的PD使血管外3 kDa葡聚糖水平升高。这些结果表明,牙周炎症诱导的IL-6表达与海马中的神经炎症和BBB破坏有关,最终导致认知障碍。牙周治疗可能预防神经退行性疾病。